EP2191820A1 - Pharmazeutische Formulierungen von Meloxicam - Google Patents

Pharmazeutische Formulierungen von Meloxicam Download PDF

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Publication number
EP2191820A1
EP2191820A1 EP09176632A EP09176632A EP2191820A1 EP 2191820 A1 EP2191820 A1 EP 2191820A1 EP 09176632 A EP09176632 A EP 09176632A EP 09176632 A EP09176632 A EP 09176632A EP 2191820 A1 EP2191820 A1 EP 2191820A1
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EP
European Patent Office
Prior art keywords
meloxicam
free solution
aqueous edta
edta free
propylene glycol
Prior art date
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Application number
EP09176632A
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English (en)
French (fr)
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EP2191820B1 (de
Inventor
Ali Turkyilmaz
Hasan Ali Turp
Cevdet Akdogan
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Sanovel Ilac Sanayi ve Ticaret AS
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Sanovel Ilac Sanayi ve Ticaret AS
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/08—Solutions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Definitions

  • This invention is a novel pharmaceutical formulation of aqueous EDTA (Ethylene diamine tetraacetic acid) free solution of meloxicam in combination with meglumin for administration by oral or parenteral route, comprising one or more pharmaceutically acceptable excipients which is comprising N,N dimethylacetamide and propylene glycol for treating mammals, preferably animals.
  • aqueous EDTA Ethylene diamine tetraacetic acid
  • aqueous EDTA free solution of meloxicam is comprising N,N dimethylacetamide and propylene glycol in a raito of between 1:2 to 1:15 (w/w). Particularly preferred ratio is 1:5 (w/w).
  • Meloxicam an oxicam derivative, is a member of the enolic acid group of nonsteroidal anti-inflammatory drugs (NSAIDs). It is reported to be a selective inhibitor of cyclooxygenase-2 (COX-2) and exerts potent anti-inflammatory, anti-rheumatismal and anti-pyretic activity.
  • NSAIDs nonsteroidal anti-inflammatory drugs
  • meloxicam is as 4-hydroxy-2-methyl- N -(5-methyl-2-thiazolyl)-2 H- 1,2-benzothiazine-3-carboxamide-1,1-dioxide and its chemical structure is shown in the Formula 1.
  • Meloxicam is a hydrophobic drug and diffucult to dissolve in aqueous solution.
  • Meglumine can increase the solubility of meloxicam in aqueous solution ( Zhao, J., Zhang, J.-S., Journal of China Pharmaceutical University, "Study on the solubilization of meloxicam in meglumine aqueous solution ", 2003, Vol.34, No.5 , abstract).
  • Meglumine is an organic base used as a pH-adjusting agent and solubilizing agent ( Handbook of pharmaceutical excipients fourth edition, Rowe, Raymond C., Sheskey, Paul J., Weller, Paul J., pages 381 and 382 ).
  • EP application EP 0 945 134 A1 (Boehringer Ingelheim Pharma KG) 27.03.1998, discloses the pH-dependent solubility characteristics of meloxicam and its salts, i.e. the sodium salt, the ammonium salt and the meglumine salt, in aqueous solution.
  • EP 1 299 107 B1 (Boehringer Ingelheim Vetmedica GmbH) 20.06.2000, relates to an aqueous cyclodextrin-free solution of meloxicam which is suitable for oral or parenteral administration, containing a pharmacologically acceptable meloxicam salt of an organic or inorganic base and one or more suitable excipients selected from EDTA, citric acid, lecithin, gluconic acid, tartaric acid and phosphoric acid or the salts thereof.
  • the formulation which contains a high concentration of active substance in a particle-free solution and is stable over the long term is suitable for treating pain, inflammation, fever, acute mastitis, diarrhoea, lameness, problems with the locomotor apparatus, and respiratory complaints in animals, preferably acute mastitis, diarrhoea, lameness, problems with the locomotor apparatus and respiratory complaints in large farm animals.
  • PCT application WO 05/105101 A1 (Boehringer Ingelheim Vetmedica GmbH) 29.04.2004, relates to use of a formulation containing meloxicam or pharmacologically acceptable meloxicam salt of an organic or inorganic base, one or more vehicles and one or more suitable additives for preparing a veterinary medical composition for intramammary treatment of inflammatory diseases in mammals, particularly mastitis.
  • PCT application WO 06/000306 A1 (Boehringer Ingelheim Vetmedica GmbH) 23.06.2004, relates to use of a formulation containing meloxicam or pharmacologically acceptable meloxicam salt of an organic or inorganic base, one or more vehicles and one or more suitable additives for preparing a veterinary medical composition for treatment of mild and/or moderate mastitis cases.
  • Meloxicam is practically insoluble in water and very slightly soluble in alcohol. Meglumine can increase the solubility of meloxicam in aqueous solution but it is not enough to derive an absolute and clear aqueous solution. In order to have this, heating process is needed or other solubilising agents are used. In prior art, a heating process at 90°C is used for preparing a pharmaceutical formulation of an aqueous solution of meloxicam.
  • EDTA is used to form stable water-soluble complexes.
  • One of the embodiments of this invention is to provide a manufacture process of stabilized aqueous EDTA free solution of meloxicam with meglumine without using the heating process for administration by oral or parenteral route, comprising one or more pharmaceutically acceptable excipients which is comprising N,N dimethylacetamide and propylene glycol.
  • This process is also environmental friendly because of its short duration and not using heating process in high degrees.
  • This invention is an aqueous EDTA free meloxicam solutions which comprise, meglumin and certain excipients, or excipient complex which is selected from the group comprising of N,N dimethylacetamide, propylene glycol, povidone, dimethyl ether, ethyl acetate, polyethylene glycol.
  • the problem underlying the present invention is to provide an aqueous EDTA free solution of meloxicam which is highly dissolved without using the heating process. Surprisingly, it has been found that, addition of N,N dimethylacetamide and propylene glycol to the present pharmaceutical formulation, an appropriate solution of meloxicam is obtained.
  • an appropriate solubility of the formulation by using the complex of N,N dimethylacetamide and propylene glycol is obtained preferably in a ratio of between 1:2 to 1:15 (w/w). Particularly preferred ratio is 1:5 (w/w).
  • aqueous EDTA free solution of meloxicam of the present invention comprising;
  • the formulation containing an aqueous medium according to the invention has a pH value in the alkaline range.
  • the meloxicam containing formulation tends to be a true aqueous solution whereas in the more acidic region it tends to be a suspension.
  • the formulation of this invention should have a pH range from 8 to 10, preferably from 8 to 9.
  • a pH value of 8 to 10 preferably from 8 to 9.
  • N,N dimethylacetamide is a basic substance and addition of meglumin and itself helped to obtain the optimum pH.
  • the pharmaceutical formulations of the invention include solutions, suspensions, any kind of injection formulations, e.g. such as intracutaneous or subcutaneous needleless injection or ready to use syringes, or injection formulations for parenteral application, such as i.v. or i.m. injection.
  • injection formulations for parenteral application such as i.v. or i.m. injection.
  • parenteral application such as i.v. or i.m. injection.
  • the preparation of pharmaceutical forms of this kind is well-known per se from the prior art.
  • solubilisers may also be used, for example propyleneglycol, polyethyleneglycols, polyoxyethylene-polyoxypropylene copolymers, propylene carbonate, polyoxyl 35 castor oil, castor oil, polysorbate, propyleneglycol monostearate, glycofurol, glycerol, sorbitol, mannitol, xylitol, povidone, N,N-dimethylacetamide and lecithin.
  • One embodiment of the invention comprises, in addition to the meloxicam in combination with meglumin, propyleneglycol, N,N-dimethylacetamide, polyvinylpyrrolidone but particularly propyleneglycol and N,N-dimethylacetamide as solubiliser.
  • the other embodiment of this invention is the preservatife use of propyleneglycol when it is used in the range of %15 to 30 ( Handbook of Pharmaceutical Excipients 4th edition, Rowe, Raymond C., Sheskey, Paul J., Weller, Paul J., pages 521-523 ).
  • sodium edetate (disodium EDTA, trisodium EDTA, tetrasodium EDTA) may cause gastrointestinal effects. Pain at the site of injection and thrombophlebitis may also occur. Other adverse effects include fever, skin rashes, hypotension and hyperuricaemia, nephrotoxicity has also been reported, particularly following overdosage. Hypocalemia can occur, particularly if sodium edetate is infused too rapidly or in too concentrated a solution and tetany, convulsions, respiratory arrest and cardiac arrhythmias may result. ( Sean C Sweetman, Martindale The Complete Drug Reference, thirty-fifth edition 2007, Vol. 1, page 1318 ) Hence it may need caution for using EDTA in highly concentrated injectable formulations.
  • the solution may have a long-term shelf-life of 24 months or more at ambient temperature, its original packaging.
  • the formulation according to the invention overcomes the problem arising from the prior art of providing an injectable solution of the active substance meloxicam in combination with meglumine comprising N,N dimethylacetamide and propylene glycol, preferably in a ratio of between 1:2 to 1:15 (w/w) and particularly preferred ratio is 1:5 (w/w) which is also suitable for treating large farm animals, by permitting a high concentration of active substance in EDTA free aqueous solution which is stable over the long term, having the formulation described hereinafter.
  • the formulation according to the invention should have a pH of between 8 and 10, preferably between 8 and 9 without using a buffer substance.
  • the formulation according to the invention is suitable for treating pain, inflammation, fever, acute mastitis, diarrhoea, lameness, problems with the locomotor apparatus and respiratory complaints in animals.
  • the treatment may be given in conjunction with antibiotic therapy.
  • the formulation according to the invention is suitable for treating mammals, preferably animals, more particularly farm animals.

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
EP09176632A 2008-12-01 2009-11-20 Pharmazeutische Formulierungen von Meloxicam Active EP2191820B1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TR2008/09200A TR200809200A1 (tr) 2008-12-01 2008-12-01 Meloksikam içeren farmasötik formülasyonlar

Publications (2)

Publication Number Publication Date
EP2191820A1 true EP2191820A1 (de) 2010-06-02
EP2191820B1 EP2191820B1 (de) 2011-09-28

Family

ID=40847870

Family Applications (1)

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EP09176632A Active EP2191820B1 (de) 2008-12-01 2009-11-20 Pharmazeutische Formulierungen von Meloxicam

Country Status (5)

Country Link
US (1) US20100137292A1 (de)
EP (1) EP2191820B1 (de)
AT (1) ATE526012T1 (de)
ES (1) ES2374626T3 (de)
TR (1) TR200809200A1 (de)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2704523B2 (de) † 2012-09-03 2019-12-18 BSH Hausgeräte GmbH Induktionskochfeldvorrichtung
CN115068419A (zh) * 2022-07-22 2022-09-20 潍坊恒邦兽药有限公司 兽用高浓度美洛昔康注射剂及其加工设备

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100297252A1 (en) 2003-03-03 2010-11-25 Elan Pharma International Ltd. Nanoparticulate meloxicam formulations
US8512727B2 (en) * 2003-03-03 2013-08-20 Alkermes Pharma Ireland Limited Nanoparticulate meloxicam formulations
US20100316725A1 (en) 2009-05-27 2010-12-16 Elan Pharma International Ltd. Reduction of flake-like aggregation in nanoparticulate active agent compositions
JOP20200109A1 (ar) 2012-04-23 2017-06-16 Otsuka Pharma Co Ltd مستحضر قابل للحقن
JP7374501B2 (ja) * 2018-05-11 2023-11-07 南京清普生物科技有限公司 メロキシカム組成物、製剤及びその製造方法と応用

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4233299A (en) 1977-12-16 1980-11-11 Boehringer Ingelheim Gmbh 4-Hydroxy-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxides and salts thereof
WO1999009988A1 (en) * 1997-08-27 1999-03-04 Hexal Ag New pharmaceutical compositions of meloxicam with improved solubility and bioavailability
EP0945134A1 (de) 1998-03-27 1999-09-29 Boehringer Ingelheim Pharma KG Neue galenische Zubereitungsformen von Meloxicam zur oralen Applikation
WO2001097813A2 (de) 2000-06-20 2001-12-27 Boehringer Ingelheim Vetmedica Gmbh Highly concentrated stable meloxicam solutions
US20020035107A1 (en) * 2000-06-20 2002-03-21 Stefan Henke Highly concentrated stable meloxicam solutions
US20030119825A1 (en) 2001-12-12 2003-06-26 Boehringer Ingelheim Vetmedica Gmbh Highly concentrated stable meloxicam solutions for needleless injection
WO2004037264A1 (de) * 2002-10-25 2004-05-06 Boehringer Ingelheim Vetmedica Gmbh Wasserlösliche meloxicam granulate
WO2005105101A1 (en) 2004-04-29 2005-11-10 Boehringer Ingelheim Vetmedica Gmbh Use of meloxicam formulations in veterinary medicine
WO2006000306A1 (en) 2004-06-23 2006-01-05 Boehringer Ingelheim Vetmedica Gmbh Use of meloxicam in veterinary medicine for the treatment of inflammatory painful diseases
US20070092539A1 (en) * 2003-07-10 2007-04-26 Arturo Jimenez-Bayardo Method of preparing an aqueous meloxicam solution and aqueous solution thus produced
WO2009156369A1 (en) 2008-06-24 2009-12-30 Intervet International B.V. Pharmaceutical transdermal compositions and method for treating inflammation in cattle

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Publication number Priority date Publication date Assignee Title
AU1548001A (en) * 1999-11-24 2001-06-04 Wakamoto Pharmaceutical Co., Ltd. Ophthalmic aqueous preparation
US8992980B2 (en) * 2002-10-25 2015-03-31 Boehringer Ingelheim Vetmedica Gmbh Water-soluble meloxicam granules
US20070281927A1 (en) * 2006-06-06 2007-12-06 Shanthakumar Tyavanagimatt Anti-inflammatory and analgesic compositions and related methods

Patent Citations (12)

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Publication number Priority date Publication date Assignee Title
US4233299A (en) 1977-12-16 1980-11-11 Boehringer Ingelheim Gmbh 4-Hydroxy-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxides and salts thereof
WO1999009988A1 (en) * 1997-08-27 1999-03-04 Hexal Ag New pharmaceutical compositions of meloxicam with improved solubility and bioavailability
EP0945134A1 (de) 1998-03-27 1999-09-29 Boehringer Ingelheim Pharma KG Neue galenische Zubereitungsformen von Meloxicam zur oralen Applikation
WO2001097813A2 (de) 2000-06-20 2001-12-27 Boehringer Ingelheim Vetmedica Gmbh Highly concentrated stable meloxicam solutions
US20020035107A1 (en) * 2000-06-20 2002-03-21 Stefan Henke Highly concentrated stable meloxicam solutions
EP1299107B1 (de) 2000-06-20 2005-06-15 Boehringer Ingelheim Vetmedica Gmbh Hochkonzentrierte stabile meloxicam-lösungen
US20030119825A1 (en) 2001-12-12 2003-06-26 Boehringer Ingelheim Vetmedica Gmbh Highly concentrated stable meloxicam solutions for needleless injection
WO2004037264A1 (de) * 2002-10-25 2004-05-06 Boehringer Ingelheim Vetmedica Gmbh Wasserlösliche meloxicam granulate
US20070092539A1 (en) * 2003-07-10 2007-04-26 Arturo Jimenez-Bayardo Method of preparing an aqueous meloxicam solution and aqueous solution thus produced
WO2005105101A1 (en) 2004-04-29 2005-11-10 Boehringer Ingelheim Vetmedica Gmbh Use of meloxicam formulations in veterinary medicine
WO2006000306A1 (en) 2004-06-23 2006-01-05 Boehringer Ingelheim Vetmedica Gmbh Use of meloxicam in veterinary medicine for the treatment of inflammatory painful diseases
WO2009156369A1 (en) 2008-06-24 2009-12-30 Intervet International B.V. Pharmaceutical transdermal compositions and method for treating inflammation in cattle

Non-Patent Citations (6)

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Title
"Veterinary Drug Handbook", UNIVERSITY PRESS, pages: 289 - 290
LUGER P ET AL: "STRUCTURE AND PHYSICOCHEMICAL PROPERTIES OF MELOXICAM, A NEW NSAID", EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, ELSEVIER, AMSTERDAM, NL, vol. 4, no. 3, 1 January 1996 (1996-01-01), pages 175 - 187, XP001179121, ISSN: 0928-0987 *
ROWE, RAYMOND C.; SHESKEY, PAUL J.; WELLER, PAUL J.: "Handbook of pharmaceutical excipients", pages: 381
ROWE, RAYMOND C.; SHESKEY, PAUL J.; WELLER, PAUL J.: "Handbook of Pharmaceutical Excipients", pages: 521 - 523
SEAN C SWEETMAN: "Martindale The Complete Drug Reference", vol. 1, 2007, pages: 1318
ZHAO, J.; ZHANG, J.-S.: "Study on the solubilization of meloxicam in meglumine aqueous solution", JOURNAL OF CHINA PHARMACEUTICAL UNIVERSITY, vol. 34, no. 5, 2003

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2704523B2 (de) † 2012-09-03 2019-12-18 BSH Hausgeräte GmbH Induktionskochfeldvorrichtung
CN115068419A (zh) * 2022-07-22 2022-09-20 潍坊恒邦兽药有限公司 兽用高浓度美洛昔康注射剂及其加工设备

Also Published As

Publication number Publication date
TR200809200A1 (tr) 2009-12-21
US20100137292A1 (en) 2010-06-03
ES2374626T3 (es) 2012-02-20
ATE526012T1 (de) 2011-10-15
EP2191820B1 (de) 2011-09-28

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